{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Redwood City",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93179",
      "recalling_firm": "Pulmonx, Corp.",
      "address_1": "700 Chesapeake Dr",
      "address_2": "",
      "postal_code": "94063-4731",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: TN, WV, AR, PA, VA, NC, IL, IA, MA, NY, NJ, WA, CO, OR, MI, FL, OH, TX, OK, AZ, NV, WI",
      "recall_number": "Z-0235-2024",
      "product_description": "Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP",
      "product_quantity": "144",
      "reason_for_recall": "Endobronchial implant devices may have been labeled with a shortened expiration date but they can be used until the correct expiration date: 08 December 2024.",
      "recall_initiation_date": "20230831",
      "center_classification_date": "20231106",
      "report_date": "20231115",
      "code_info": "UDI: (01)00811907030423(10)506590V70(17)241208, Lot: 506590-V7.0",
      "more_code_info": ""
    }
  ]
}